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10339-62-5

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10339-62-5 Usage

General Description

Trans-4-Decen-1-ol, also known as 4-decenol, is a long-chain unsaturated alcohol with the chemical formula C10H20O. It is a colorless liquid with a sweet, floral, and waxy odor. Trans-4-Decen-1-OL is used primarily as a flavoring agent in the food and beverage industry, particularly in the production of fruit and floral flavors. It is also used in the formulation of perfumes and fragrances due to its pleasant aroma. Additionally, trans-4-decen-1-ol has potential applications as a surfactant or emulsifier in cosmetic and personal care products. Furthermore, it may have antimicrobial properties and could be used as an ingredient in pharmaceutical products. However, further research is needed to fully understand and exploit its potential benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 10339-62-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,3 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 10339-62:
(7*1)+(6*0)+(5*3)+(4*3)+(3*9)+(2*6)+(1*2)=75
75 % 10 = 5
So 10339-62-5 is a valid CAS Registry Number.

10339-62-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (4E)-4-Decen-1-ol

1.2 Other means of identification

Product number -
Other names 4-Decenoic acid,(4E)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:10339-62-5 SDS

10339-62-5Relevant articles and documents

Selective deoxygenation of allylic alcohol: Stereocontrolled synthesis of lavandulol

Kim, Hee Jin,Su, Liang,Jung, Heejung,Koo, Sangho

, p. 2682 - 2685 (2011/06/26)

Selective deoxygenation of allylic alcohol can be successfully carried out by the formation of alkoxyalkyl ether (EE or MOM), followed by Pd(dppe)Cl 2-catalyzed reduction with LiBHEt3. (+)-S-Lavandulol has been efficiently synthesized by the application of this protocol to the diol derived from the Pb(OAc)4-promoted oxidative ring-opening of (-)-R-carvone. This deoxygenation method is general and selective for allylic alcohols.

Dihydrogen reduction of carboxylic esters to alcohols under the catalysis of homogeneous ruthenium complexes: High efficiency and unprecedented chemoselectivity

Saudan, Lionel A.,Saudan, Christophe M.,Debieux, Catherine,Wyss, Patrick

, p. 7473 - 7476 (2008/09/18)

(Chemical Equation Presented) The missing link: The presence of two N,P bridges in the ruthenium complexes used as catalysts for the title reaction is essential. Esters that contain isolated C=C bonds are reduced to the corresponding unsaturated alcohols in high yields with high chemoselectivity (see example).

REGIOSELECTIVE HYDROALUMINATION OF UNSATURATED HYDROCARBONS BY ALKYLALANES CATALYZED BY ZIRCONIUM COMPLEXES

Dzhemilev, U. M.,Ibragimov, A. G.,Vostrikova, O. S.,Vasil'eva, E. V.,Tolstikov, G. A.

, p. 1004 - 1009 (2007/10/02)

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